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Girl with no face facial deformities

Ms Hall had a further 18 operations over the next 14 years, including facelifts, rhinoplasty, skin grafts, liposuction, dermabrasion, eye surgery and laser surgery. Ms Hall, who now works on a surgical ward at Kettering General Hospital, suffered years of painful procedures as surgeons reconstructed her face. You can find our Community Guidelines in full here. Want to discuss real-world problems, be involved in the most engaging discussions and hear from the journalists?
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'The girl with half a face': Teen with rare facial deformity opens up in new documentary

Girl with no face facial deformities
Girl with no face facial deformities
Girl with no face facial deformities
Girl with no face facial deformities
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Why the mom of a child with a facial deformity fought to take down just one cruel tweet - CNN

When Angel was born, her mother Cypres Salon, from the Philippines, was concerned when she didn't hear her daughter cry. But it wasn't until she saw her baby for the first time five days later, that she realised the severity of the situation. Little Angel had been rushed to another hospital for treatment after being born with encephalocele, a rare brain hernia. The hernia, which is more common in children from South-East Asia than elsewhere, is caused when the skull and tissue surrounding the brain doesn't completely close up in the womb. Angel, four, from the Philippines, was rushed to another hospital for treatment shortly after being born after being diagnosed with encephalocele, a rare brain hernia. Angel was also labelled a 'monster' by her peers but when a four-year-old boy approached her and said it to her face, the optimistic little girl simply 'patted him on the shoulder and said "Hi".
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Sophia Weaver, girl cyber-bullied for facial deformities, dies at age 10

Sarah Atwell in the hall of her high school. Surviving adolescence can be difficult for anyone — but for Sarah Atwell, navigating her teenage years was an especially harsh struggle. Since birth, Sarah has suffered from a rare disease called neurofibromatosis — a condition that triggered a massive tumor to develop on half of her face.
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The account that was using my daughter's image has been suspended! Thank you for taking a stand against hate! Chat with us in Facebook Messenger.
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